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FDAOctober 17, 2022device

Arrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/AJLA, REF IAP-0701 (IPN917286), cardiac pump

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

2080190217207920801902172072

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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